Reaktion #46265

ord-5b677e9021ef49aa8905e2820f0536ce

Reaktionsgleichung

O
water
CCCCOC(=O)CNC(=O)C(=O)OCC
butyl N-[ethoxy(oxo)acetyl]glycinate
O=P12OP3(=O)OP(=O)(O1)OP(=O)(O2)O3
phosphorus pentoxide
CCCCOc1cnc(C(=O)OCC)o1
title material
CCCCOc1cnc(C(=O)OCC)o1
Ethyl 5-butoxy-1,3-oxazole-2-carboxylate

Lösungsmittel

Reaktionsbedingungen

Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe product mixture was cooled
  2. 2
    Temperaturmaintained at 20° C
  3. 3
    ExtraktionThe resultant mixture was extracted with dichloromethane (8 L, and 3 times 2 L)
  4. 4
    Waschenwashed twice with saturated aqueous sodium bicarbonate (8 L total)
  5. 5
    Trocknendried over anhydrous magnesium sulfate
  6. 6
    Filtrationfiltered
  7. 7
    Einengenconcentrated under vacuum
  8. 8
    SonstigeCollection and concentration of appropriate fractions

Vorschrift

To a solution of butyl N-[ethoxy(oxo)acetyl]glycinate (783 g, 3.38 mol) in acetonitrile (8 L) in a 50 L glass reactor with overhead stirrer, phosphorus pentoxide (415 g, 2.92 mol) was added in portions. The reaction was heated at 60° C. for 1 hour. The product mixture was cooled, and water (8 L) was added with the mixture maintained at 20° C. The resultant mixture was extracted with dichloromethane (8 L, and 3 times 2 L). The organic extracts were combined, washed twice with saturated aqueous sodium bicarbonate (8 L total), dried over anhydrous magnesium sulfate, filtered and concentrated under vacuum. The residual oil was subjected to column chromatography on silica gel eluting with 0-30% heptane/ethyl acetate gradient. Collection and concentration of appropriate fractions provided the title material.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07741315B2uspto-grants-2010_06